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3-chloro-5-hydroxy BA

3-氯-5-羟基苯甲酸
Catalog No.
C3411
GPR81激动剂
组合的产品项目
规格价格库存 数量
10mM (in 1mL DMSO)
¥ 454.00
现货
50mg
¥ 567.00
现货
100mg
¥ 1,063.00
现货
500mg
¥ 4,632.00
Ship with 10-15 days

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A

背景

3-chloro-5-hydroxy BA is a GPR81 agonist.

GPR81 (HCA1) is a member of G-protein-coupled receptors (GPCRs). GPR81 is predominantly expressed on adipocytes and is activated by the endogenous ligands 2-hydroxypropanoate (lactate). Stimulation of GPR81 in adipose tissue lead to a decrease in the lipolysis of triglycerides by hormone-sensitive lipase, which resulted in reduced transport of fatty acids to the liver and a decrease in hepatic triglycerides [1].

In vitro: In the hGPR81 assay, 3-chloro-5-hydroxybenzoic acid showed the potency against GPR81 with an EC50 of 16 μM. The EC50 of 3-chloro-5-hydroxybenzoic acid against monkey GPR81, dog GPR81, rat GPR81, mouse GPR81, and hamster GPR81 was 17 μM, 67 μM, 7 μM, 22 μM and 27 μM, respectively [1]. 3-chloro-5-hydroxy BA blocked basal ghrelin secretion by primary gastric mucosal cells [2].

In vivo: In mice, oral administration of 3-chloro-5-hydroxybenzoic acid at 30 mg/kg provided a Cmax of 67 μM at approximately 3-fold over the in vitro EC50 with an AUCinf of 54 h μM and a short t1/2 of 1.5 h, and the 100 mg/kg p.o dose attained a Cmax of 342 μM at greater than 15-fold over the observed in vitro EC50 [1].

References:
[1].  Dvorak C A, Liu C, Shelton J, et al. Identification of hydroxybenzoic acids as selective lactate receptor (GPR81) agonists with antilipolytic effects[J]. ACS medicinal chemistry letters, 2012, 3(8): 637-639.
[2].  Engelstoft M S, Park W, Sakata I, et al. Seven transmembrane G protein-coupled receptor repertoire of gastric ghrelin cells[J]. Molecular metabolism, 2013, 2(4): 376-392.

文献引用

化学属性

StorageStore at -20°C
M.Wt172.6
Cas No.53984-36-4
FormulaC7H5ClO3
Synonyms3-chloro-5-hydroxy BA,CHBA,GPR81 Agonist
Solubilityinsoluble in H2O; ≥52.2 mg/mL in EtOH; ≥6.65 mg/mL in DMSO
Chemical Name3-chloro-5-hydroxy-benzoic acid
SDFDownload SDF
Canonical SMILESClC1=CC(O)=CC(C(O)=O)=C1
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